
Bioorganic and Medicinal Chemistry p. 2747 - 2761 (2012)
Update date:2022-08-03
Topics:
Nie, Yong-Yan
Da, Ya-Jing
Zheng, Hao
Yang, Xiao-Xia
Jia, Lin
Wen, Cai-Hong
Liang, Li-Sha
Tian, Juan
Chen, Zhi-Long
A series of novel angiotensin II type 1 receptor antagonists were prepared. Radioligand binding assay suggested that compounds 1b and 1c could be recognized by the AT1 receptor with an IC50 value of 1.6 ± 0.09 nM and 2.64 ± 0.7 nM, respectively. In vivo anti-hypertension experiments showed that compounds (1a, 1b, 1c, 1e) elicited a significant decrease in SBP and DBP of spontaneous hypertensive rats (SHRs). The antihypertensive effects maintained for 10 h, which indicated that these compounds had a favorable blood pressure-lowering effect. Acute toxicity testing suggested that the LD50 value of compound 1b was 2316.8 mg/kg which was lower than valsartan (LD50 = 307.50 mg/kg) but higher than losartan (LD50 = 2248 mg/kg). So they could be considered as novel anti-hypertension candidates and deserved for further investigation.
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